6-74192297-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192297
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192297
    reference: chr 6
allele count: 1
allele frequency: 8.297791128001726e-6
allele num: 120514
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1613T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.256T>C
  hgvsp: ENST00000521156.1:c.256T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.239T>C
  hgvsp: ENST00000523763.1:c.239T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1666T>C
  hgvsp: ENST00000370300.4:c.1666T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1772T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1711T>C
  hgvsp: ENST00000415954.2:c.1711T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*722T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1591T>C
  hgvsp: ENST00000498286.1:c.1591T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1444T>C
  hgvsp: ENST00000370305.1:c.1444T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*69T>C
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14728
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5712
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu571Leu
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

6-74192309-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192309
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192309
    reference: chr 6
allele count: 1
allele frequency: 8.323483877411729e-6
allele num: 120142
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1456G>A
  hgvsp: ENSP00000359328.1:p.Ala486Thr
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.268G>A
  hgvsp: ENSP00000428863.1:p.Ala90Thr
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1678G>A
  hgvsp: ENSP00000359323.4:p.Ala560Thr
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1625G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*81G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1784G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.251G>A
  hgvsp: ENSP00000429595.1:p.Ala85Thr
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1603G>A
  hgvsp: ENSP00000419561.1:p.Ala535Thr
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1723G>A
  hgvsp: ENSP00000402038.2:p.Ala575Thr
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*734G>A
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala575Thr
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ

6-74192310-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192310
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192310
    reference: chr 6
allele count: 1
allele frequency: 8.323206765102459e-6
allele num: 120146
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*82C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.252C>T
  hgvsp: ENSP00000429595.1:p.Ala85Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1457C>T
  hgvsp: ENSP00000359328.1:p.Ala486Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1785C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1604C>T
  hgvsp: ENSP00000419561.1:p.Ala535Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1679C>T
  hgvsp: ENSP00000359323.4:p.Ala560Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*735C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.269C>T
  hgvsp: ENSP00000428863.1:p.Ala90Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1724C>T
  hgvsp: ENSP00000402038.2:p.Ala575Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1626C>T
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala575Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

6-74192315-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192315
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192315
    reference: chr 6
allele count: 11
allele frequency: 9.168806054746107e-5
allele num: 119972
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*87A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.257A>G
  hgvsp: ENSP00000429595.1:p.Ile87Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.274A>G
  hgvsp: ENSP00000428863.1:p.Ile92Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1729A>G
  hgvsp: ENSP00000402038.2:p.Ile577Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*740A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1790A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1462A>G
  hgvsp: ENSP00000359328.1:p.Ile488Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1631A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1684A>G
  hgvsp: ENSP00000359323.4:p.Ile562Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1609A>G
  hgvsp: ENSP00000419561.1:p.Ile537Val
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36260
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14667
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile577Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

6-74192320-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192320
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192320
    reference: chr 6
allele count: 1
allele frequency: 8.34306691139663e-6
allele num: 119860
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1636T>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1689T>G
  hgvsp: ENSP00000359323.4:p.Ser563Arg
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*745T>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*92T>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.279T>G
  hgvsp: ENSP00000428863.1:p.Ser93Arg
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1734T>G
  hgvsp: ENSP00000402038.2:p.Ser578Arg
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1614T>G
  hgvsp: ENSP00000419561.1:p.Ser538Arg
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1467T>G
  hgvsp: ENSP00000359328.1:p.Ser489Arg
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1795T>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.262T>G
  hgvsp: ENSP00000429595.1:p.Ser88Arg
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36201
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14635
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser578Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/6-74192322-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192322
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192322
    reference: chr 6
allele count: 7
allele frequency: 5.843364442292602e-5
allele num: 119794
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1616C>A
  hgvsp: ENSP00000419561.1:p.Thr539Asn
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1638C>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.281C>A
  hgvsp: ENSP00000428863.1:p.Thr94Asn
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1691C>A
  hgvsp: ENSP00000359323.4:p.Thr564Asn
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1469C>A
  hgvsp: ENSP00000359328.1:p.Thr490Asn
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*94C>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1736C>A
  hgvsp: ENSP00000402038.2:p.Thr579Asn
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.264C>A
  hgvsp: ENSP00000429595.1:p.Thr89Asn
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*747C>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1797C>A
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5621
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr579Asn
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

6-74192325-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192325
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192325
    reference: chr 6
allele count: 1
allele frequency: 8.36050497450046e-6
allele num: 119610
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1800G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1641G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1694G>A
  hgvsp: ENSP00000359323.4:p.Ser565Asn
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1619G>A
  hgvsp: ENSP00000419561.1:p.Ser540Asn
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*97G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.267G>A
  hgvsp: ENSP00000429595.1:p.Ser90Asn
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1739G>A
  hgvsp: ENSP00000402038.2:p.Ser580Asn
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*750G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1472G>A
  hgvsp: ENSP00000359328.1:p.Ser491Asn
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.284G>A
  hgvsp: ENSP00000428863.1:p.Ser95Asn
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14607
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser580Asn
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP

6-74192325-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192325
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192325
    reference: chr 6
allele count: 2
allele frequency: 1.672100994900092e-5
allele num: 119610
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1694G>T
  hgvsp: ENSP00000359323.4:p.Ser565Ile
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*750G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1619G>T
  hgvsp: ENSP00000419561.1:p.Ser540Ile
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1739G>T
  hgvsp: ENSP00000402038.2:p.Ser580Ile
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.267G>T
  hgvsp: ENSP00000429595.1:p.Ser90Ile
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1472G>T
  hgvsp: ENSP00000359328.1:p.Ser491Ile
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1800G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*97G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1641G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.284G>T
  hgvsp: ENSP00000428863.1:p.Ser95Ile
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1451
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser580Ile
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

6-74192326-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192326
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192326
    reference: chr 6
allele count: 1
allele frequency: 8.360784576024614e-6
allele num: 119606
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1695T>C
  hgvsp: ENST00000370300.4:c.1695T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1620T>C
  hgvsp: ENST00000498286.1:c.1620T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.268T>C
  hgvsp: ENST00000523763.1:c.268T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*98T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.285T>C
  hgvsp: ENST00000521156.1:c.285T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1801T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1473T>C
  hgvsp: ENST00000370305.1:c.1473T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1740T>C
  hgvsp: ENST00000415954.2:c.1740T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*751T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1642T>C
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser580Ser
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

6-74192327-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192327
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192327
    reference: chr 6
allele count: 1
allele frequency: 8.36344172353807e-6
allele num: 119568
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*99A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1802A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1741A>G
  hgvsp: ENSP00000402038.2:p.Arg581Gly
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1474A>G
  hgvsp: ENSP00000359328.1:p.Arg492Gly
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*752A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1696A>G
  hgvsp: ENSP00000359323.4:p.Arg566Gly
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.286A>G
  hgvsp: ENSP00000428863.1:p.Arg96Gly
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1621A>G
  hgvsp: ENSP00000419561.1:p.Arg541Gly
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.269A>G
  hgvsp: ENSP00000429595.1:p.Arg91Gly
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1643A>G
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14613
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg581Gly
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: A
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

6-74192332-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192332
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192332
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 119196
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*104T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1701T>C
  hgvsp: ENST00000370300.4:c.1701T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1626T>C
  hgvsp: ENST00000498286.1:c.1626T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1807T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1648T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*757T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1746T>C
  hgvsp: ENST00000415954.2:c.1746T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.274T>C
  hgvsp: ENST00000523763.1:c.274T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.291T>C
  hgvsp: ENST00000521156.1:c.291T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1479T>C
  hgvsp: ENST00000370305.1:c.1479T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1663
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser582Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

6-74192339-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192339
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192339
    reference: chr 6
allele count: 1
allele frequency: 8.453799983092399e-6
allele num: 118290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1655G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1633G>A
  hgvsp: ENSP00000419561.1:p.Val545Ile
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*111G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.281G>A
  hgvsp: ENSP00000429595.1:p.Val95Ile
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1814G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1708G>A
  hgvsp: ENSP00000359323.4:p.Val570Ile
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.298G>A
  hgvsp: ENSP00000428863.1:p.Val100Ile
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1753G>A
  hgvsp: ENSP00000402038.2:p.Val585Ile
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*764G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1486G>A
  hgvsp: ENSP00000359328.1:p.Val496Ile
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2222
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Val585Ile
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

6-74192343-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192343
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192343
    reference: chr 6
allele count: 2
allele frequency: 1.698081168279844e-5
allele num: 117780
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1659G>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1490G>C
  hgvsp: ENSP00000359328.1:p.Arg497Thr
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.302G>C
  hgvsp: ENSP00000428863.1:p.Arg101Thr
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1712G>C
  hgvsp: ENSP00000359323.4:p.Arg571Thr
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1757G>C
  hgvsp: ENSP00000402038.2:p.Arg586Thr
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1637G>C
  hgvsp: ENSP00000419561.1:p.Arg546Thr
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*115G>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1818G>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*768G>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.285G>C
  hgvsp: ENSP00000429595.1:p.Arg96Thr
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg586Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

6-74192346-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192346
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192346
    reference: chr 6
allele count: 1
allele frequency: 8.530239699735563e-6
allele num: 117230
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1490+3A>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.302+3A>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1757+3A>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*768+3A>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*115+3A>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1659+3A>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1637+3A>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1818+3A>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.285+3A>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1712+3A>T
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13760
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1757+3A>T
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

6-74192348-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192348
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192348
    reference: chr 6
allele count: 1
allele frequency: 8.541314337450248e-6
allele num: 117078
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.285+5G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1757+5G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1712+5G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1659+5G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1818+5G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1637+5G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*115+5G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1490+5G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.302+5G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*768+5G>A
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13710
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1757+5G>A
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-74192350-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192350
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192350
    reference: chr 6
allele count: 2
allele frequency: 1.715089356155456e-5
allele num: 116612
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*768+7A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1490+7A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1637+7A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1757+7A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.285+7A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.302+7A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*115+7A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1818+7A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1712+7A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1659+7A>G
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13446
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32314
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.1757+7A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum

6-74192357-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192357
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192357
    reference: chr 6
allele count: 1
allele frequency: 8.643490587238751e-6
allele num: 115694
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.302+14A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1490+14A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1712+14A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1757+14A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.285+14A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*768+14A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*115+14A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1818+14A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1659+14A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1637+14A>G
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5576
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2219
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38969
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

6-74192359-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192359
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192359
    reference: chr 6
allele count: 57
allele frequency: 4.94062581260293e-4
allele num: 115370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1818+16A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1757+16A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*115+16A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.302+16A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1637+16A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1659+16A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.285+16A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1712+16A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1490+16A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*768+16A>G
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6212
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12518
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29902
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 3.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 1358
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

6-74192364-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192364
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192364
    reference: chr 6
allele count: 1
allele frequency: 8.744622057434678e-6
allele num: 114356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*115+21C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1818+21C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1757+21C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1637+21C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1490+21C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.302+21C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.285+21C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1659+21C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*768+21C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1712+21C>T
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11808
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1470
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35108
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

6-74192365-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192365
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192365
    reference: chr 6
allele count: 1
allele frequency: 8.799718409010911e-6
allele num: 113640
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.302+22C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1712+22C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*768+22C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1637+22C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1659+22C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1757+22C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.285+22C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*115+22C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1818+22C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1490+22C>G
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25839
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9623
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11220
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2458
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1446
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum

6-74192379-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192379
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192379
    reference: chr 6
allele count: 4
allele frequency: 3.616963559092142e-5
allele num: 110590
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.285+36A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1757+36A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*768+36A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.302+36A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1659+36A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1490+36A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1712+36A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1818+36A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*115+36A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1637+36A>G
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12762
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8459
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1009
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

6-74192386-AATAAGATC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74192386
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74192378
    reference: chr 6
allele count: 1
allele frequency: 9.189149452326692e-6
allele num: 108824
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15267
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4691
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13649
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7457
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14362
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2217
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: AATAAGATC
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

6-74196289-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74196289
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74196289
    reference: chr 6
allele count: 2
allele frequency: 2.990430622009569e-4
allele num: 6688
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*768+3946C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1757+3946C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.302+3946C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1637+3946C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.286-32C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1659+3946C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1490+3946C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1818+3946C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*115+3946C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1712+3946C>T
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

6-74196290-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74196290
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74196290
    reference: chr 6
allele count: 1007
allele frequency: 1.434881732687375e-1
allele num: 7018
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1712+3947G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1637+3947G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.286-31G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1818+3947G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1659+3947G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*115+3947G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1757+3947G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.302+3947G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1490+3947G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*768+3947G>A
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 7.5e0
  variant carriers: 219
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 2.5e0
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 1.75e1
  variant carriers: 374
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 2.25e1
  variant carriers: 143
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 2.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 1.25e1
  variant carriers: 366
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 6.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 1659
  bin: 2.25e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 8.25e1
  variant carriers: 25
num of homozygotes: 76
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

6-74196311-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74196311
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74196311
    reference: chr 6
allele count: 1
allele frequency: 1.481042654028436e-4
allele num: 6752
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1712+3968A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*115+3968A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.286-10A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1490+3968A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1818+3968A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1637+3968A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1659+3968A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1757+3968A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.302+3968A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*768+3968A>G
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2388
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

6-74196336-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74196336
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74196336
    reference: chr 6
allele count: 1
allele frequency: 1.636125654450262e-4
allele num: 6112
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1757+3993T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1818+3993T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.302+3993T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1490+3993T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1712+3993T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1659+3993T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*768+3993T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1637+3993T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.301T>C
  hgvsp: ENST00000523763.1:c.301T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*115+3993T>C
  variant of: http://identifiers.org/hgnc/19261
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
hgvs: p.His101His
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

6-74196376-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74196376
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74196376
    reference: chr 6
allele count: 1
allele frequency: 2.57201646090535e-4
allele num: 3888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1659+4033G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1757+4033G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*768+4033G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1490+4033G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*115+4033G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1712+4033G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.341G>A
  hgvsp: ENSP00000429595.1:p.Val115Ile
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.302+4033G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1637+4033G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1818+4033G>A
  variant of: http://identifiers.org/hgnc/19261
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 1.25e1
  variant carriers: 1
hgvs: p.Val115Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum

6-74196409-CGA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74196409
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74196407
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 1096
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1637+4069_1637+4070delGA
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.302+4069_302+4070delGA
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*768+4069_*768+4070delGA
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1757+4069_1757+4070delGA
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1659+4069_1659+4070delGA
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*31_*32delGA
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1818+4069_1818+4070delGA
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1712+4069_1712+4070delGA
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*115+4069_*115+4070delGA
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1490+4069_1490+4070delGA
  variant of: http://identifiers.org/hgnc/19261
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2704
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: CGA
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

6-74201917-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201917
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201917
    reference: chr 6
allele count: 1
allele frequency: 8.279379377721846e-6
allele num: 120782
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1819-40C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*116-40C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*104-40C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.201G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.303-40C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*769-40C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1758-40C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1491-40C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1638-40C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1660-40C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1713-40C>G
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ

6-74201917-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201917
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201917
    reference: chr 6
allele count: 18
allele frequency: 1.490288287989932e-4
allele num: 120782
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*769-40C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.303-40C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1758-40C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*104-40C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1713-40C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1819-40C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1660-40C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1638-40C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.201G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1491-40C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*116-40C>T
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2442
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27300
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9329
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

6-74201919-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201919
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201919
    reference: chr 6
allele count: 7
allele frequency: 5.794030493154767e-5
allele num: 120814
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.303-38T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1713-38T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*116-38T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*104-38T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1660-38T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1819-38T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.199A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1638-38T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1758-38T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*769-38T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1491-38T>C
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14179
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9302
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27448
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

6-74201920-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201920
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201920
    reference: chr 6
allele count: 1
allele frequency: 8.278282753025713e-6
allele num: 120798
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1758-37G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.198C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1638-37G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*769-37G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*116-37G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.303-37G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1491-37G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1660-37G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1819-37G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*104-37G>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1713-37G>A
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14239
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27474
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

6-74201929-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201929
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201929
    reference: chr 6
allele count: 1
allele frequency: 8.272667107875579e-6
allele num: 120880
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1758-28T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1660-28T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.189A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*104-28T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*769-28T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1713-28T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1638-28T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.303-28T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1819-28T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1491-28T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*116-28T>C
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS

http://identifiers.org/exac.variant/6-74201937-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201937
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201937
    reference: chr 6
allele count: 1
allele frequency: 8.269520202437855e-6
allele num: 120926
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*104-20A>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1819-20A>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.303-20A>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*116-20A>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1638-20A>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.181T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1660-20A>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1491-20A>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*769-20A>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1758-20A>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1713-20A>C
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9267
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15218
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-74201940-CTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201940
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201938
    reference: chr 6
allele count: 3
allele frequency: 2.480445818795165e-5
allele num: 120946
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.303-15_303-14delTT
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1713-15_1713-14delTT
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1491-15_1491-14delTT
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*116-15_*116-14delTT
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1819-15_1819-14delTT
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1638-15_1638-14delTT
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.176_177delAA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*104-15_*104-14delTT
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1758-15_1758-14delTT
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1660-15_1660-14delTT
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*769-15_*769-14delTT
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9275
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15318
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: CTT
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

6-74201943-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201943
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201943
    reference: chr 6
allele count: 1
allele frequency: 8.265692417053776e-6
allele num: 120982
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*104-14T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1660-14T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*769-14T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1819-14T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1638-14T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.175A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*116-14T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1491-14T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1713-14T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.303-14T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1758-14T>C
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ

6-74201945-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201945
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201945
    reference: chr 6
allele count: 4
allele frequency: 3.305621208865676e-5
allele num: 121006
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*104-12A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.173T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1713-12A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1491-12A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*116-12A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.303-12A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1660-12A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1819-12A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1638-12A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*769-12A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1758-12A>G
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15479
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

6-74201947-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201947
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201947
    reference: chr 6
allele count: 2
allele frequency: 1.652428243303535e-5
allele num: 121034
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*104-10A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1713-10A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*116-10A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.303-10A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1660-10A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.171T>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1758-10A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1819-10A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1491-10A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1638-10A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*769-10A>G
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum

6-74201959-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201959
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201959
    reference: chr 6
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1760C>T
  hgvsp: ENSP00000402038.2:p.Ala587Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*771C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1640C>T
  hgvsp: ENSP00000419561.1:p.Ala547Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1662C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1493C>T
  hgvsp: ENSP00000359328.1:p.Ala498Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*118C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*106C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1715C>T
  hgvsp: ENSP00000359323.4:p.Ala572Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1821C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.159G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.305C>T
  hgvsp: ENSP00000428863.1:p.Ala102Val
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala587Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

6-74201961-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201961
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201961
    reference: chr 6
allele count: 9
allele frequency: 7.426845571124424e-5
allele num: 121182
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1717C>G
  hgvsp: ENSP00000359323.4:p.Leu573Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*773C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1762C>G
  hgvsp: ENSP00000402038.2:p.Leu588Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.157G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1642C>G
  hgvsp: ENSP00000419561.1:p.Leu548Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1495C>G
  hgvsp: ENSP00000359328.1:p.Leu499Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.307C>G
  hgvsp: ENSP00000428863.1:p.Leu103Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*120C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1664C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*108C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1823C>G
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9288
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15749
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28309
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu588Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD

6-74201969-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201969
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201969
    reference: chr 6
allele count: 2
allele frequency: 1.649620587264929e-5
allele num: 121240
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*116T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1650T>C
  hgvsp: ENST00000498286.1:c.1650T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.149A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.315T>C
  hgvsp: ENST00000521156.1:c.315T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1672T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*781T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1770T>C
  hgvsp: ENST00000415954.2:c.1770T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*128T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1503T>C
  hgvsp: ENST00000370305.1:c.1503T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1725T>C
  hgvsp: ENST00000370300.4:c.1725T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1831T>C
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15743
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28412
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val590Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

6-74201972-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201972
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201972
    reference: chr 6
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1773G>T
  hgvsp: ENST00000415954.2:c.1773G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1653G>T
  hgvsp: ENST00000498286.1:c.1653G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1728G>T
  hgvsp: ENST00000370300.4:c.1728G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.146C>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.318G>T
  hgvsp: ENST00000521156.1:c.318G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*784G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1506G>T
  hgvsp: ENST00000370305.1:c.1506G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1675G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1834G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*131G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*119G>T
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu591Leu
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

6-74201974-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201974
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201974
    reference: chr 6
allele count: 4
allele frequency: 3.299077907724791e-5
allele num: 121246
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1836A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*786A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1508A>G
  hgvsp: ENSP00000359328.1:p.Lys503Arg
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*121A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.320A>G
  hgvsp: ENSP00000428863.1:p.Lys107Arg
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1775A>G
  hgvsp: ENSP00000402038.2:p.Lys592Arg
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.144T>C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*133A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1730A>G
  hgvsp: ENSP00000359323.4:p.Lys577Arg
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1655A>G
  hgvsp: ENSP00000419561.1:p.Lys552Arg
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1677A>G
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28445
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys592Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ

6-74201977-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201977
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201977
    reference: chr 6
allele count: 2
allele frequency: 1.649457328538911e-5
allele num: 121252
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.323A>G
  hgvsp: ENSP00000428863.1:p.Tyr108Cys
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*136A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*789A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1778A>G
  hgvsp: ENSP00000402038.2:p.Tyr593Cys
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1680A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1839A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1658A>G
  hgvsp: ENSP00000419561.1:p.Tyr553Cys
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.141T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1733A>G
  hgvsp: ENSP00000359323.4:p.Tyr578Cys
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1511A>G
  hgvsp: ENSP00000359328.1:p.Tyr504Cys
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*124A>G
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr593Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

6-74201985-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201985
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201985
    reference: chr 6
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1519G>T
  hgvsp: ENSP00000359328.1:p.Val507Phe
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1688G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1786G>T
  hgvsp: ENSP00000402038.2:p.Val596Phe
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*144G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.331G>T
  hgvsp: ENSP00000428863.1:p.Val111Phe
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*132G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1741G>T
  hgvsp: ENSP00000359323.4:p.Val581Phe
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1847G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*797G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1666G>T
  hgvsp: ENSP00000419561.1:p.Val556Phe
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.133C>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val596Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

6-74201986-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201986
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201986
    reference: chr 6
allele count: 15
allele frequency: 1.236888976845438e-4
allele num: 121272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1667T>C
  hgvsp: ENSP00000419561.1:p.Val556Ala
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*798T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1689T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1520T>C
  hgvsp: ENSP00000359328.1:p.Val507Ala
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1742T>C
  hgvsp: ENSP00000359323.4:p.Val581Ala
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1787T>C
  hgvsp: ENSP00000402038.2:p.Val596Ala
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1848T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.332T>C
  hgvsp: ENSP00000428863.1:p.Val111Ala
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*145T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*133T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.132A>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9287
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Val596Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

6-74201988-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201988
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201988
    reference: chr 6
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1669G>T
  hgvsp: ENSP00000419561.1:p.Asp557Tyr
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*800G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*147G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.130C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1522G>T
  hgvsp: ENSP00000359328.1:p.Asp508Tyr
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1691G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1744G>T
  hgvsp: ENSP00000359323.4:p.Asp582Tyr
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1789G>T
  hgvsp: ENSP00000402038.2:p.Asp597Tyr
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.334G>T
  hgvsp: ENSP00000428863.1:p.Asp112Tyr
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*135G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1850G>T
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28501
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp597Tyr
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD

6-74201989-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201989
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201989
    reference: chr 6
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*136A>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1692A>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*148A>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1790A>T
  hgvsp: ENSP00000402038.2:p.Asp597Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.335A>T
  hgvsp: ENSP00000428863.1:p.Asp112Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1670A>T
  hgvsp: ENSP00000419561.1:p.Asp557Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.129T>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1745A>T
  hgvsp: ENSP00000359323.4:p.Asp582Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1523A>T
  hgvsp: ENSP00000359328.1:p.Asp508Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*801A>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1851A>T
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9283
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp597Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

6-74201994-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201994
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201994
    reference: chr 6
allele count: 1
allele frequency: 8.244838730954422e-6
allele num: 121288
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.340G>T
  hgvsp: ENSP00000428863.1:p.Asp114Tyr
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*141G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*153G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1528G>T
  hgvsp: ENSP00000359328.1:p.Asp510Tyr
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.124C>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*806G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1750G>T
  hgvsp: ENSP00000359323.4:p.Asp584Tyr
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1795G>T
  hgvsp: ENSP00000402038.2:p.Asp599Tyr
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1675G>T
  hgvsp: ENSP00000419561.1:p.Asp559Tyr
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1697G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1856G>T
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9287
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15727
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28536
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp599Tyr
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP

6-74201995-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74201995
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74201995
    reference: chr 6
allele count: 2
allele frequency: 1.648967746190884e-5
allele num: 121288
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.341A>G
  hgvsp: ENSP00000428863.1:p.Asp114Gly
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*154A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1796A>G
  hgvsp: ENSP00000402038.2:p.Asp599Gly
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1529A>G
  hgvsp: ENSP00000359328.1:p.Asp510Gly
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.123T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1698A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1751A>G
  hgvsp: ENSP00000359323.4:p.Asp584Gly
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1857A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*807A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1676A>G
  hgvsp: ENSP00000419561.1:p.Asp559Gly
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*142A>G
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp599Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

6-74202015-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74202015
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74202015
    reference: chr 6
allele count: 3
allele frequency: 2.473981956424931e-5
allele num: 121262
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*827C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1696C>G
  hgvsp: ENSP00000419561.1:p.Pro566Ala
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.361C>G
  hgvsp: ENSP00000428863.1:p.Pro121Ala
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1549C>G
  hgvsp: ENSP00000359328.1:p.Pro517Ala
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1816C>G
  hgvsp: ENSP00000402038.2:p.Pro606Ala
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*174C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1877C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.103G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1771C>G
  hgvsp: ENSP00000359323.4:p.Pro591Ala
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*162C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1718C>G
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro606Ala
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD

6-74202021-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74202021
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74202021
    reference: chr 6
allele count: 1
allele frequency: 8.247014580721778e-6
allele num: 121256
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1702C>G
  hgvsp: ENSP00000419561.1:p.Pro568Ala
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1777C>G
  hgvsp: ENSP00000359323.4:p.Pro593Ala
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*180C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1822C>G
  hgvsp: ENSP00000402038.2:p.Pro608Ala
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.367C>G
  hgvsp: ENSP00000428863.1:p.Pro123Ala
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1555C>G
  hgvsp: ENSP00000359328.1:p.Pro519Ala
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.97G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1883C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*833C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1724C>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*168C>G
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28583
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9280
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro608Ala
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-74202024-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74202024
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74202024
    reference: chr 6
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.370T>C
  hgvsp: ENST00000521156.1:c.370T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*836T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*183T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1780T>C
  hgvsp: ENST00000370300.4:c.1780T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1825T>C
  hgvsp: ENST00000415954.2:c.1825T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1886T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1705T>C
  hgvsp: ENST00000498286.1:c.1705T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1558T>C
  hgvsp: ENST00000370305.1:c.1558T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*171T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.94A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1727T>C
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15615
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu609Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

6-74202026-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74202026
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74202026
    reference: chr 6
allele count: 1
allele frequency: 8.248511143738554e-6
allele num: 121234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1782G>T
  hgvsp: ENSP00000359323.4:p.Leu594Phe
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.92C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.372G>T
  hgvsp: ENSP00000428863.1:p.Leu124Phe
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1707G>T
  hgvsp: ENSP00000419561.1:p.Leu569Phe
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1888G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1827G>T
  hgvsp: ENSP00000402038.2:p.Leu609Phe
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*173G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1729G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1560G>T
  hgvsp: ENSP00000359328.1:p.Leu520Phe
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*838G>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*185G>T
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15610
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9277
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu609Phe
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

6-74202035-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74202035
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74202035
    reference: chr 6
allele count: 1
allele frequency: 8.254911672445104e-6
allele num: 121140
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1791T>C
  hgvsp: ENST00000370300.4:c.1791T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1716T>C
  hgvsp: ENST00000498286.1:c.1716T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*182T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1569T>C
  hgvsp: ENST00000370305.1:c.1569T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*194T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.381T>C
  hgvsp: ENST00000521156.1:c.381T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.83A>G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1836T>C
  hgvsp: ENST00000415954.2:c.1836T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1738T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1897T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*847T>C
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9267
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr612Tyr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

6-74202036-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74202036
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74202036
    reference: chr 6
allele count: 1
allele frequency: 8.254911672445104e-6
allele num: 121140
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*183A>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000430660
  ensembl transcript: ENST00000524046
  gene symbol: MTO1
  hgvsc: ENST00000524046.1:c.*195A>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1898A>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1739A>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1570A>T
  hgvsp: ENSP00000359328.1:p.Thr524Ser
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1717A>T
  hgvsp: ENSP00000419561.1:p.Thr573Ser
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1837A>T
  hgvsp: ENSP00000402038.2:p.Thr613Ser
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.382A>T
  hgvsp: ENSP00000428863.1:p.Thr128Ser
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*848A>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1792A>T
  hgvsp: ENSP00000359323.4:p.Thr598Ser
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.82T>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9267
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr613Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

6-74202049-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74202049
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74202049
    reference: chr 6
allele count: 1
allele frequency: 8.268426187759421e-6
allele num: 120942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1752A>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.69T>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*861A>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1730A>T
  hgvsp: ENSP00000419561.1:p.Glu577Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1583A>T
  hgvsp: ENSP00000359328.1:p.Glu528Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.395A>T
  hgvsp: ENSP00000428863.1:p.Glu132Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*196A>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1805A>T
  hgvsp: ENSP00000359323.4:p.Glu602Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1850A>T
  hgvsp: ENSP00000402038.2:p.Glu617Val
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1911A>T
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Glu617Val
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

6-74202094-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74202094
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74202094
    reference: chr 6
allele count: 1
allele frequency: 8.469551960701279e-6
allele num: 118070
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1876+19C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1778+19C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1831+19C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1609+19C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1756+19C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1937+19C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*222+19C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.421+19C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*887+19C>T
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.56-32G>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6686
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23103
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11576
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4471
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1320
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

6-74202106-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74202106
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74202106
    reference: chr 6
allele count: 2
allele frequency: 1.700391089950689e-5
allele num: 117620
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*222+31T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1609+31T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1876+31T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1778+31T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.56-44A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.421+31T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1937+31T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1756+31T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*887+31T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1831+31T>C
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9365
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1918
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

6-74202111-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74202111
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74202111
    reference: chr 6
allele count: 1
allele frequency: 8.532132009146445e-6
allele num: 117204
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1937+36A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1778+36A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.421+36A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*222+36A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*887+36A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1876+36A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1756+36A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1831+36A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1609+36A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.56-49T>C
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12898
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9735
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9120
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5670
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4451
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

6-74202114-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74202114
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74202114
    reference: chr 6
allele count: 1
allele frequency: 8.543649505322693e-6
allele num: 117046
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*222+39T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*887+39T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1876+39T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1778+39T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.56-52A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1831+39T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1609+39T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1937+39T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.421+39T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1756+39T>C
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9744
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13727
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4130
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

6-74202125-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74202125
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74202125
    reference: chr 6
allele count: 1
allele frequency: 8.649321893163576e-6
allele num: 115616
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1756+50T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*887+50T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1831+50T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.421+50T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.56-63A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1778+50T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1609+50T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1937+50T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*222+50T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1876+50T>C
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 9510
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13803
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6483
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1192
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1291
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum

6-74202126-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74202126
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74202126
    reference: chr 6
allele count: 3
allele frequency: 2.603398302584307e-5
allele num: 115234
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1876+51G>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000223821
  ensembl transcript: ENST00000423099
  gene symbol: RP11-505P4.6
  hgvsc: ENST00000423099.1:n.56-64C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1609+51G>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*887+51G>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1937+51G>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1756+51G>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1778+51G>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.421+51G>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*222+51G>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1831+51G>C
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13916
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15096
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7967
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

6-74207412-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74207412
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74207412
    reference: chr 6
allele count: 1
allele frequency: 8.332361224523806e-6
allele num: 120014
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1938-47A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1832-47A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1779-47A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.422-2885A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1877-47A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*223-2885A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1757-47A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1610-47A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*888-47A>G
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3699
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 804
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3486
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1192
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

6-74207417-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74207417
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74207417
    reference: chr 6
allele count: 1
allele frequency: 8.328197611472925e-6
allele num: 120074
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1779-42A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*888-42A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*223-2880A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1832-42A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1938-42A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1877-42A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1757-42A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.422-2880A>G
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1610-42A>G
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7742
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2005
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3486
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

6-74207418-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74207418
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74207418
    reference: chr 6
allele count: 1
allele frequency: 8.325008325008325e-6
allele num: 120120
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1832-41T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*888-41T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1779-41T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1877-41T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1610-41T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*223-2879T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.422-2879T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1938-41T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1757-41T>C
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8335
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16616
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2084
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

6-74207421-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74207421
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74207421
    reference: chr 6
allele count: 10
allele frequency: 8.324176738920521e-5
allele num: 120132
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1938-38T>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1877-38T>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*888-38T>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1757-38T>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1610-38T>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.422-2876T>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*223-2876T>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1779-38T>A
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1832-38T>A
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25718
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17382
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8305
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2005
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7794
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

6-74207428-ATT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74207428
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74207426
    reference: chr 6
allele count: 1
allele frequency: 8.314487162431821e-6
allele num: 120272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.422-2868_422-2867delTT
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000402038
  ensembl transcript: ENST00000415954
  gene symbol: MTO1
  hgvsc: ENST00000415954.2:c.1877-30_1877-29delTT
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1779-30_1779-29delTT
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1757-30_1757-29delTT
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1938-30_1938-29delTT
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*223-2868_*223-2867delTT
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*888-30_*888-29delTT
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359323
  ensembl transcript: ENST00000370300
  gene symbol: MTO1
  hgvsc: ENST00000370300.4:c.1832-30_1832-29delTT
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1610-30_1610-29delTT
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: ATT
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-74207432-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74207432
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 74207432
    reference: chr 6
allele count: 1
allele frequency: 8.303992559622666e-6
allele num: 120424
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000419561
  ensembl transcript: ENST00000498286
  gene symbol: MTO1
  hgvsc: ENST00000498286.1:c.1757-27T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000370308
  gene symbol: MTO1
  hgvsc: ENST00000370308.4:n.1938-27T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl transcript: ENST00000462039
  gene symbol: MTO1
  hgvsc: ENST00000462039.1:n.1779-27T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000428863
  ensembl transcript: ENST00000521156
  gene symbol: MTO1
  hgvsc: ENST00000521156.1:c.422-2865T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000429595
  ensembl transcript: ENST00000523763
  gene symbol: MTO1
  hgvsc: ENST00000523763.1:c.*223-2865T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000416397
  ensembl transcript: ENST00000415228
  gene symbol: MTO1
  hgvsc: ENST00000415228.1:c.*888-27T>C
  variant of: http://identifiers.org/hgnc/19261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000135297
  ensembl protein: ENSP00000359328
  ensembl transcript: ENST00000370305
  gene symbol: MTO1
  hgvsc: ENST00000370305.1:c.1610-27T>C
  variant of: http://identifiers.org/hgnc/19261
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 1598
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1458
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46745
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2226
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 41
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10054
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.166044776119403e-4
allele num: 8576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66394
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.732e1

MQRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.246e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.21e0

DP
type: SiteQuality
SIO_000300: 1.532644e6

GenotypeQuality
all individuals: 1456
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2225
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 52
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 854
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 46524
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1589
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5675
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.008064516129032e-4
allele num: 9920
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66234
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16418
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.006e0

QD
type: SiteQuality
SIO_000300: 7.48e0

MQRankSum
type: SiteQuality
SIO_000300: 3.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

DP
type: SiteQuality
SIO_000300: 1.528328e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 88
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5669
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1588
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46561
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1453
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2225
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 931
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509753004408479e-5
allele num: 66236
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9924
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.121e0

VQSLOD
type: SiteQuality
SIO_000300: -8.219e-1

DP
type: SiteQuality
SIO_000300: 1.528472e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.051e0

QD
type: SiteQuality
SIO_000300: 1.046e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e0

FS
type: SiteQuality
SIO_000300: 2.039e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 999
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46440
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1585
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5656
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2234
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1455
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66154
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.497861942577886e-4
allele num: 16370
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.022244691607685e-4
allele num: 9890
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

FS
type: SiteQuality
SIO_000300: 1.192e0

DP
type: SiteQuality
SIO_000300: 1.526079e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.69e0

MQRankSum
type: SiteQuality
SIO_000300: -1.28e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e-1

QD
type: SiteQuality
SIO_000300: 1.291e1

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5632
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2223
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 56
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1453
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 46349
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1580
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1081
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66110
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9856
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.116956202593589e-5
allele num: 16348
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.985e1

VQSLOD
type: SiteQuality
SIO_000300: 5.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.76e-1

DP
type: SiteQuality
SIO_000300: 1.523966e6

MQRankSum
type: SiteQuality
SIO_000300: 5.21e-1

FS
type: SiteQuality
SIO_000300: 2.67e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.73e-1

QD
type: SiteQuality
SIO_000300: 1.559e1

GenotypeQuality
all individuals: 1128
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2229
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1573
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1453
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 929
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46265
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9852
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.059289973063769e-4
allele num: 66082
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.523534e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.031e0

FS
type: SiteQuality
SIO_000300: 3.58e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.57e-1

QD
type: SiteQuality
SIO_000300: 1.137e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.75e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

MQRankSum
type: SiteQuality
SIO_000300: -1.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.84e-1

GenotypeQuality
all individuals: 159
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2224
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1573
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1294
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5622
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45984
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1451
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16268
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65982
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.697164724299878e-5
allele num: 11498
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.72e-1

QD
type: SiteQuality
SIO_000300: 1.038e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.936e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.519e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-1

FS
type: SiteQuality
SIO_000300: 4.539e0

MQ
type: SiteQuality
SIO_000300: 5.898e1

DP
type: SiteQuality
SIO_000300: 1.520331e6

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2224
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 45984
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9830
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16268
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.03112970203995e-5
allele num: 65982
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.936e-1

FS
type: SiteQuality
SIO_000300: 4.539e0

MQ
type: SiteQuality
SIO_000300: 5.898e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.519e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

DP
type: SiteQuality
SIO_000300: 1.520331e6

QD
type: SiteQuality
SIO_000300: 1.038e1

GenotypeQuality
all individuals: 161
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5614
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.697164724299878e-5
allele num: 11498
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9828
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16264
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65984
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.12e0

FS
type: SiteQuality
SIO_000300: 7.638e0

DP
type: SiteQuality
SIO_000300: 1.520325e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.183e0

VQSLOD
type: SiteQuality
SIO_000300: 3.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.46e-1

QD
type: SiteQuality
SIO_000300: 1.075e1

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1449
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
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variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1572
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variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2222
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 46032
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5621
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 921
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65960
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.153088850603002e-5
allele num: 16252
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9828
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.519315e6

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 4.091e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.331e0

MQRankSum
type: SiteQuality
SIO_000300: -3.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.113e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.33e-1

QD
type: SiteQuality
SIO_000300: 1.171e1

GenotypeQuality
all individuals: 488
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45573
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2221
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1565
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5589
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65758
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9784
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16140
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.14e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.504e0

DP
type: SiteQuality
SIO_000300: 1.513427e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 9.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.06e-1

GenotypeQuality
all individuals: 116
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1542
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44436
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65362
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.031140441328109e-4
allele num: 9698
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15782
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.56e0

DP
type: SiteQuality
SIO_000300: 1.49754e6

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

MQ
type: SiteQuality
SIO_000300: 5.826e1

FS
type: SiteQuality
SIO_000300: 3.459e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 9.460000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

VQSLOD
type: SiteQuality
SIO_000300: -2.03e0

GenotypeDepth
all individuals: 826
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2223
bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.361275088547816e-4
allele num: 8470
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65124
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9646
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.484603e6

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

MQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

QD
type: SiteQuality
SIO_000300: 1.256e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

FS
type: SiteQuality
SIO_000300: 4.878e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.387e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 484
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variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64868
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.03950103950104e-4
allele num: 9620
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15386
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.386e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.749e0

FS
type: SiteQuality
SIO_000300: 4.478e0

DP
type: SiteQuality
SIO_000300: 1.469983e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.72e0

QD
type: SiteQuality
SIO_000300: 9.67e0

GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8440
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.525711302531976e-5
allele num: 15324
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64798
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.2821e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

BaseQRankSum
type: SiteQuality
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DP
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -5.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.51e-1

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64594
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8424
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.087246921310791e-4
allele num: 9582
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15128
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.56e-1

DP
type: SiteQuality
SIO_000300: 1.453439e6

VQSLOD
type: SiteQuality
SIO_000300: -4.45e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.21e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 5.132e0

QD
type: SiteQuality
SIO_000300: 1.245e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9530
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8390
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14780
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.558409175913228e-5
allele num: 64168
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11384
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.68e-1

DP
type: SiteQuality
SIO_000300: 1.423157e6

FS
type: SiteQuality
SIO_000300: 2.2484e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.09e-1

QD
type: SiteQuality
SIO_000300: 1.514e1

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.58e0

VQSLOD
type: SiteQuality
SIO_000300: -3.415e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.522997258604935e-4
allele num: 6566
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 8.359207069500836e-4
allele num: 8374
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14666
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.152073732718894e-3
allele num: 868
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.791981712678038e-5
allele num: 11374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 47
allele frequency: 7.341455795064043e-4
allele num: 64020
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.957e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.27e-1

VQSLOD
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SIO_000300: 2.01e0

ClippingRankSum
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
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QD
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SIO_000300: 1.413e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11334
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.574803149606299e-5
allele num: 63500
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.618e0

InbreedingCoeff
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VQSLOD
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DP
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MQ
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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SIO_000300: 5.34e-1

ClippingRankSum
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QD
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63110
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Latino
type: Population
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Other
type: Population
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele num: 14172
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
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FS
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VQSLOD
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QD
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DP
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.865390853065196e-5
allele num: 61660
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8182
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6544
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South Asian
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 830
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele count: 1
allele frequency: 1.08837614279495e-4
allele num: 9188
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.337e1

MQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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FS
type: SiteQuality
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BaseQRankSum
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.69e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9136
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60792
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.116883116883117e-5
allele num: 12320
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8088
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11142
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.081e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e-1

MQ
type: SiteQuality
SIO_000300: 5.246e1

DP
type: SiteQuality
SIO_000300: 1.200767e6

VQSLOD
type: SiteQuality
SIO_000300: 1.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 6.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.15e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 60
num of homozygotes: 0

South Asian
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allele frequency: 4.34593654932638e-4
allele num: 4602
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -8.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
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SIO_000300: 0.0e0

DP
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InbreedingCoeff
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SIO_000300: -3.31e-2

VQSLOD
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QD
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SIO_000300: 1.228e1

MQ
type: SiteQuality
SIO_000300: 5.812e1

MQRankSum
type: SiteQuality
SIO_000300: -3.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.86e-1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 732

GenotypeQuality
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bin: 6.25e1
variant carriers: 35

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 405
allele frequency: 2.230176211453745e-1
allele num: 1816
num of homozygotes: 39

Other
type: Population
allele count: 10
allele frequency: 1.25e-1
allele num: 80
num of homozygotes: 2

Latino
type: Population
allele count: 6
allele frequency: 9.677419354838709e-2
allele num: 62
num of homozygotes: 0

African
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allele count: 15
allele frequency: 1.027397260273973e-1
allele num: 146
num of homozygotes: 2

East Asian
type: Population
allele count: 1
allele frequency: 7.936507936507936e-3
allele num: 126
num of homozygotes: 0

South Asian
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allele count: 570
allele frequency: 1.19047619047619e-1
allele num: 4788
num of homozygotes: 33

FS
type: SiteQuality
SIO_000300: 1.192e0

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

DP
type: SiteQuality
SIO_000300: 7.7082e4

InbreedingCoeff
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SIO_000300: 5.83e-2

MQ
type: SiteQuality
SIO_000300: 5.637e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.3e-2

QD
type: SiteQuality
SIO_000300: 1.294e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.53e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.149613069647464e-4
allele num: 4652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 150
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1690
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.29e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 5.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
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SIO_000300: -1.214e0

MQ
type: SiteQuality
SIO_000300: 5.883e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.12e0

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.67e-1

DP
type: SiteQuality
SIO_000300: 7.9272e4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1482
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.354048964218456e-4
allele num: 4248
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 120
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ClippingRankSum
type: SiteQuality
SIO_000300: 7.17e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.43e-1

MQ
type: SiteQuality
SIO_000300: 5.912e1

FS
type: SiteQuality
SIO_000300: 2.463e0

ReadPosRankSum
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SIO_000300: -1.186e0

InbreedingCoeff
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SIO_000300: -3.42e-2

DP
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SIO_000300: 7.4562e4

VQSLOD
type: SiteQuality
SIO_000300: -1.626e0

BaseQRankSum
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SIO_000300: 2.64e0

QD
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SIO_000300: 8.630000000000001e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 3.759398496240602e-4
allele num: 2660
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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FS
type: SiteQuality
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MQ
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QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: 7.4e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
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allele num: 0
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Latino
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allele count: 0
allele frequency: 0.0e0
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South Asian
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East Asian
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allele frequency: 0.0e0
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Other
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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MQ
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ClippingRankSum
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ReadPosRankSum
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QD
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FS
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VQSLOD
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DP
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

Latino
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66542
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South Asian
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European (Finnish)
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Other
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MQRankSum
type: SiteQuality
SIO_000300: -1.66e-1

DP
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FS
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 18

African
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allele frequency: 9.852216748768474e-5
allele num: 10150
num of homozygotes: 0

South Asian
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East Asian
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allele count: 17
allele frequency: 1.971700301554164e-3
allele num: 8622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66542
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.122e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

FS
type: SiteQuality
SIO_000300: 1.681e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.369e0

DP
type: SiteQuality
SIO_000300: 1.750045e6

GenotypeQuality
all individuals: 611
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 732
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37080
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7792
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1519
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4204
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 877
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2221
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2534
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 3.469210754553339e-4
allele num: 11530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10154
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.508295263284443e-5
allele num: 66544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.02e-1

DP
type: SiteQuality
SIO_000300: 1.751087e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -3.659e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.71e-1

FS
type: SiteQuality
SIO_000300: 9.835000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.38e0

QD
type: SiteQuality
SIO_000300: 1.145e1

GenotypeQuality
all individuals: 618
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37400
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7770
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2514
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
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variant carriers: 0

GenotypeQuality
all individuals: 243
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GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 7.5e0
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GenotypeQuality
all individuals: 2215
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 605
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variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 871
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4196
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 466
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66530
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10156
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.073120369245719e-5
allele num: 16466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.901e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.223e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.774e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.36e-2

QD
type: SiteQuality
SIO_000300: 5.21e0

FS
type: SiteQuality
SIO_000300: 1.999e0

DP
type: SiteQuality
SIO_000300: 1.752253e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.85e0

MQRankSum
type: SiteQuality
SIO_000300: 2.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4195
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7722
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38845
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2454
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2155
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1483
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10180
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66570
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.069434328720563e-5
allele num: 16476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.53e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.788e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.41e-1

DP
type: SiteQuality
SIO_000300: 1.757431e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

QD
type: SiteQuality
SIO_000300: 9.029999999999999e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4191
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 144
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7700
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
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variant carriers: 0

GenotypeQuality
all individuals: 39615
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variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2141
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1461
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2414
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.792401096748923e-5
allele num: 10212
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66574
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

DP
type: SiteQuality
SIO_000300: 1.762443e6

MQRankSum
type: SiteQuality
SIO_000300: 9.53e-1

QD
type: SiteQuality
SIO_000300: 1.453e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.12e-1

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 7696
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 39853
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 2408
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variant carriers: 0

GenotypeQuality
all individuals: 179
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variant carriers: 0

GenotypeQuality
all individuals: 134
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variant carriers: 0

GenotypeQuality
all individuals: 4193
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1462
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2132
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 856
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.505857614899369e-5
allele num: 66580
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.992e1

FS
type: SiteQuality
SIO_000300: 3.476e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.32e-1

DP
type: SiteQuality
SIO_000300: 1.763955e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.88e-1

QD
type: SiteQuality
SIO_000300: 2.075e1

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40121
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 7692
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variant carriers: 0

GenotypeQuality
all individuals: 593
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variant carriers: 0

GenotypeQuality
all individuals: 2405
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variant carriers: 0

GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 4191
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 192
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GenotypeQuality
all individuals: 2139
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variant carriers: 0

GenotypeQuality
all individuals: 264
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variant carriers: 0

GenotypeQuality
all individuals: 137
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variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1464
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GenotypeQuality
all individuals: 856
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variant carriers: 0

GenotypeQuality
all individuals: 194
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variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501681883709755e-5
allele num: 66592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10236
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.94e0

DP
type: SiteQuality
SIO_000300: 1.765165e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-2

QD
type: SiteQuality
SIO_000300: 1.387e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.79e-1

FS
type: SiteQuality
SIO_000300: 8.81e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.934e-1

MQ
type: SiteQuality
SIO_000300: 5.744e1

GenotypeQuality
all individuals: 89
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 158
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GenotypeQuality
all individuals: 4190
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variant carriers: 4

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 82
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GenotypeQuality
all individuals: 116
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GenotypeQuality
all individuals: 594
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GenotypeQuality
all individuals: 40240
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GenotypeQuality
all individuals: 165
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GenotypeQuality
all individuals: 136
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GenotypeQuality
all individuals: 241
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GenotypeQuality
all individuals: 2405
bin: 7.75e1
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GenotypeQuality
all individuals: 119
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GenotypeQuality
all individuals: 2134
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GenotypeQuality
all individuals: 7696
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1462
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variant carriers: 0

GenotypeQuality
all individuals: 855
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.006186371963122e-5
allele num: 66598
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10242
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.23e-2

DP
type: SiteQuality
SIO_000300: 1.76632e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.21e-1

FS
type: SiteQuality
SIO_000300: 2.531e0

QD
type: SiteQuality
SIO_000300: 1.191e1

VQSLOD
type: SiteQuality
SIO_000300: 5.95e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.56e-1

MQ
type: SiteQuality
SIO_000300: 5.922e1

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
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GenotypeQuality
all individuals: 102
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 100
bin: 2.75e1
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GenotypeQuality
all individuals: 146
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4186
bin: 9.75e1
variant carriers: 2

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10256
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.315886984715146e-4
allele num: 8636
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.84e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

DP
type: SiteQuality
SIO_000300: 1.767309e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-2

QD
type: SiteQuality
SIO_000300: 1.245e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e0

VQSLOD
type: SiteQuality
SIO_000300: 5.84e-1

FS
type: SiteQuality
SIO_000300: 1.928e0

MQ
type: SiteQuality
SIO_000300: 5.92e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.58e-1

GenotypeDepth
all individuals: 137
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 109
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variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
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GenotypeQuality
all individuals: 71
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1454
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2395
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500375093773443e-5
allele num: 66650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

DP
type: SiteQuality
SIO_000300: 1.771861e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

FS
type: SiteQuality
SIO_000300: 1.062e0

VQSLOD
type: SiteQuality
SIO_000300: -3.834e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.343e0

MQRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.414e0

QD
type: SiteQuality
SIO_000300: 8.9e0

GenotypeQuality
all individuals: 139
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7682
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 9

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 40929
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2134
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000390050706592e-5
allele num: 66658
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.423654871546292e-4
allele num: 16504
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.732501732501733e-4
allele num: 11544
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.76e-1

DP
type: SiteQuality
SIO_000300: 1.772238e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.7e-1

FS
type: SiteQuality
SIO_000300: 1.852e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

QD
type: SiteQuality
SIO_000300: 1.413e1

GenotypeQuality
all individuals: 7686
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 592
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variant carriers: 0

GenotypeQuality
all individuals: 110
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variant carriers: 0

GenotypeQuality
all individuals: 1452
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 4182
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
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GenotypeQuality
all individuals: 2148
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variant carriers: 0

GenotypeQuality
all individuals: 2394
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999850007499625e-5
allele num: 66670
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.44e-1

QD
type: SiteQuality
SIO_000300: 1.268e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.954e1

FS
type: SiteQuality
SIO_000300: 1.118e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.61e0

MQRankSum
type: SiteQuality
SIO_000300: 9.53e-1

DP
type: SiteQuality
SIO_000300: 1.773454e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.12e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 111
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4179
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513775355737209e-4
allele num: 6606
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.587e0

MQ
type: SiteQuality
SIO_000300: 5.874e1

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

FS
type: SiteQuality
SIO_000300: 6.823e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.31e-1

QD
type: SiteQuality
SIO_000300: 1.458e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.43e-1

DP
type: SiteQuality
SIO_000300: 1.773726e6

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.423948612289419e-4
allele num: 16502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.22e-1

QD
type: SiteQuality
SIO_000300: 1.106e1

FS
type: SiteQuality
SIO_000300: 1.0665e1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.9e-2

BaseQRankSum
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SIO_000300: 2.48e0

DP
type: SiteQuality
SIO_000300: 1.773826e6

MQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999760019198464e-5
allele num: 66672
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.23e0

MQ
type: SiteQuality
SIO_000300: 5.913e1

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.205e0

DP
type: SiteQuality
SIO_000300: 1.774018e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.52e-1

QD
type: SiteQuality
SIO_000300: 1.391e1

ReadPosRankSum
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SIO_000300: 4.21e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 850
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variant carriers: 0

GenotypeQuality
all individuals: 1446
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499610101373643e-5
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Latino
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East Asian
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European (Finnish)
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South Asian
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InbreedingCoeff
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VQSLOD
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MQ
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MQRankSum
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DP
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FS
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ClippingRankSum
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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Other
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East Asian
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African
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South Asian
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European (Non-Finnish)
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MQ
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MQRankSum
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FS
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Finnish)
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East Asian
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European (Non-Finnish)
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Other
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DP
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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MQRankSum
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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Other
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African
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European (Non-Finnish)
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Latino
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MQ
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ClippingRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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DP
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VQSLOD
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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African
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Latino
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East Asian
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European (Finnish)
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InbreedingCoeff
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BaseQRankSum
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QD
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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VQSLOD
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FS
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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Latino
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Other
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European (Non-Finnish)
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South Asian
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East Asian
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QD
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MQ
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InbreedingCoeff
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FS
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BaseQRankSum
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ClippingRankSum
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DP
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VQSLOD
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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Other
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Latino
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European (Non-Finnish)
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East Asian
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European (Finnish)
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ReadPosRankSum
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MQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQ
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DP
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Finnish)
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East Asian
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European (Non-Finnish)
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DP
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QD
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ClippingRankSum
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FS
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InbreedingCoeff
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MQRankSum
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MQ
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VQSLOD
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SIO_000300: 1.53e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.68e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.13e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157407407407407e-4
allele num: 8640
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10352
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Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.92e-1

InbreedingCoeff
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MQ
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SIO_000300: 5.876e1

MQRankSum
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QD
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DP
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VQSLOD
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.101e0

FS
type: SiteQuality
SIO_000300: 1.092e0

ClippingRankSum
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SIO_000300: -1.477e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499745043342632e-5
allele num: 66678
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.8e-2

BaseQRankSum
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MQ
type: SiteQuality
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DP
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MQRankSum
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SIO_000300: -1.26e-1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e-2

QD
type: SiteQuality
SIO_000300: 1.15e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

South Asian
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allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.941e1

MQRankSum
type: SiteQuality
SIO_000300: -5.56e-1

BaseQRankSum
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DP
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 7.075e0

VQSLOD
type: SiteQuality
SIO_000300: -6.992e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e-1

QD
type: SiteQuality
SIO_000300: 8.08e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.252e1

MQ
type: SiteQuality
SIO_000300: 5.848e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503216884132043e-5
allele num: 66524
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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QD
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 8.898380494749955e-5
allele num: 11238
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9968
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64822
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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BaseQRankSum
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InbreedingCoeff
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MQ
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FS
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DP
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

African
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allele frequency: 1.010917913465427e-4
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 64602
num of homozygotes: 0

East Asian
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allele count: 0
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Latino
type: Population
allele count: 1
allele frequency: 8.941344778254649e-5
allele num: 11184
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.525441e6

VQSLOD
type: SiteQuality
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BaseQRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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FS
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ClippingRankSum
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ReadPosRankSum
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QD
type: SiteQuality
SIO_000300: 1.153e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

South Asian
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allele count: 1
allele frequency: 6.218132073125233e-5
allele num: 16082
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11152
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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FS
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InbreedingCoeff
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SIO_000300: 2.0e-4

VQSLOD
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QD
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ClippingRankSum
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MQ
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MQRankSum
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
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allele frequency: 0.0e0
allele num: 8310
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64272
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 9834
num of homozygotes: 0

Latino
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allele frequency: 8.983111749910169e-5
allele num: 11132
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

MQ
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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FS
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BaseQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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SIO_000300: 4.52e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 63436
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 6.282196255811031e-5
allele num: 15918
num of homozygotes: 0

DP
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SIO_000300: 1.409576e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.051e0

InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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MQRankSum
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MQ
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FS
type: SiteQuality
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QD
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BaseQRankSum
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SIO_000300: -2.764e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8150
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9708
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.74939049488649e-5
allele num: 63166
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15904
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10912
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.114e1

MQRankSum
type: SiteQuality
SIO_000300: -8.35e-1

ReadPosRankSum
type: SiteQuality
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MQ
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SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -8.0e-4

BaseQRankSum
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SIO_000300: 1.67e0

VQSLOD
type: SiteQuality
SIO_000300: 5.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.4e-1

DP
type: SiteQuality
SIO_000300: 1.408672e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10158
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15886
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.507840772014475e-5
allele num: 66320
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.262e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.25e-1

BaseQRankSum
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SIO_000300: 4.98e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.649999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.647888e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele frequency: 6.279829188646068e-5
allele num: 15924
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66336
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele count: 0
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 2.76e-1

ClippingRankSum
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ReadPosRankSum
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QD
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MQRankSum
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 2.151e0

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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East Asian
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
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QD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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DP
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MQ
type: SiteQuality
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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South Asian
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Other
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European (Non-Finnish)
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African
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East Asian
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InbreedingCoeff
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QD
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ReadPosRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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MQ
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DP
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VQSLOD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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type: Population
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num of homozygotes: 0

Latino
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African
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East Asian
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allele num: 8614
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European (Finnish)
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South Asian
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European (Non-Finnish)
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QD
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MQ
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MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.91e-1

DP
type: SiteQuality
SIO_000300: 1.678801e6

FS
type: SiteQuality
SIO_000300: 3.159e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.91e-1